Maintenance Planner & EAMS Administrator

What You Will Achieve In this role, you will: • Engage in planning and coordination activities to facilitate preventive maintenance, calibration & corrective maintenance (repairs). Develop & communicate maintenance schedules to effectively utilize resources. • Support manufacturing, packaging, laboratory, EHS, quality operations and engineering teams by scheduling maintenance work and communicating effectively. Attend routine scheduling meetings. • Responsible for reviewing & closing preventive maintenance and corrective work orders. • Responsible for planning/scheduling maintenance & engineering activities for plant shutdowns. • Responsible for supporting Maintenance/Engineering related safety initiatives, investigations & corrective actions. • Develops and identifies continuous improvement opportunities and leads cross-functional projects. • Coordinate/schedule contracted support and oversight as necessary. • Support general facility maintenance including pest control management, grounds maintenance and facility repairs. • Assist with maintenance/engineering PM instruction revision, execution, extension, and/or archival.   Here Is What You Need (Minimum Requirements) • Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience • Proficient computer skills in Microsoft office (word, excel, power point, etc.), CMMS (computerized maintenance management system), and other relevant software. • Strong written and verbal communication skills • Ability to facilitate cross-functional meetings effectively • Effective time management skills   Bonus Points If You Have (Preferred Requirements) • Experience working in a pharmaceutical or medical device manufacturing environment. • Knowledge and experience with continuous improvement change implementation • Familiarity with planning and execution of maintenance tasks and activities • Ability to manage multiple tasks simultaneously • General knowledge of GMP and GDP requirements • Experience working in a regulated industry (i.e. FDA, OSHA, etc.) • Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. PHYSICAL/MENTAL REQUIREMENTS • This is an on-site role at a penicillin manufacturing facility.  Candidate must not be allergic to penicillin. • Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and complex data analysis, problem solving.  • Ability to work in clean room conditions.  • Requires good planning, organizing, time management and team participation skills. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS • Standard (M-F) daytime.  Overtime work may be required. Work requires on-site presence. Non-Regular Work Schedule: • At different times of the year, this position will work long hours for scheduled manufacturing shutdown periods. • Although this is primarily a first shift role, candidate must be willing to work weekends and off shifts to support planned and unplanned production outages as need arises when equipment is unexpectedly down.  Work Location Assignment: On Premise     The annual base salary for this position ranges from $68,600.00 to $114,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacati